Authors:
TERRIS B
MEDDEB M
MARCHIO A
DANGLOT G
FLEJOU JF
BELGHITI J
RUSZNIEWSKI P
BERNHEIM A
Citation: B. Terris et al., COMPARATIVE GENOMIC HYBRIDIZATION ANALYSIS OF SPORADIC NEUROENDOCRINETUMORS OF THE DIGESTIVE-SYSTEM, Genes, chromosomes & cancer, 22(1), 1998, pp. 50-56
Authors:
MARCHIO A
MEDDEB M
PINEAU P
DANGLOT G
TIOLLAIS P
BERNHEIM A
DEJEAN A
Citation: A. Marchio et al., RECURRENT CHROMOSOMAL-ABNORMALITIES IN HEPATOCELLULAR-CARCINOMA DETECTED BY COMPARATIVE GENOMIC HYBRIDIZATION, Genes, chromosomes & cancer, 18(1), 1997, pp. 59-65
Citation: A. Valent et al., MAPPING OF THE TYROSINE KINASE RECEPTORS TRKA (NTRK1), TRKB (NTRK2) AND TRKC (NTRK3) TO HUMAN-CHROMOSOMES 1Q22, 9Q22 AND 15Q25 BY FLUORESCENCE IN-SITU HYBRIDIZATION, European journal of human genetics, 5(2), 1997, pp. 102-104
Authors:
REGNIER V
MEDDEB M
LECOINTRE G
RICHARD F
DUVERGER A
NGUYEN VG
DUTRILLAUX B
BERNHEIM A
DANGLOT G
Citation: V. Regnier et al., EMERGENCE AND SCATTERING OF MULTIPLE NEUROFIBROMATOSIS (NF1)-RELATED SEQUENCES DURING HOMINOID EVOLUTION SUGGEST A PROCESS OF PERICENTROMERIC INTERCHROMOSOMAL TRANSPOSITION, Human molecular genetics, 6(1), 1997, pp. 9-16
Authors:
MEDDEB M
DANGLOT G
CHUDOBA I
VENUAT AM
BENARD J
AVETLOISEAU H
VASSEUR B
LEPASLIER D
TERRIERLACOMBE MJ
HARTMANN O
BERNHEIM A
Citation: M. Meddeb et al., ADDITIONAL COPIES OF A 25 MB CHROMOSOMAL REGION ORIGINATING FROM 17Q23.1-17QTER ARE PRESENT IN 90-PERCENT OF HIGH-GRADE NEUROBLASTOMAS, Genes, chromosomes & cancer, 17(3), 1996, pp. 156-165
Authors:
MEDDEB M
VALENT A
DANGLOT G
NGUYEN VC
DUVERGER A
FOUQUET F
TERRIERLACOMBE MJ
OBERLIN O
BERNHEIM A
Citation: M. Meddeb et al., MDM2 AMPLIFICATION IN A PRIMARY ALVEOLAR RHABDOMYOSARCOMA DISPLAYING A T(2-13)(Q35-Q14), Cytogenetics and cell genetics, 73(4), 1996, pp. 325-330
Authors:
GOGUEL AF
PULCINI F
DANGLOT G
FAUVET D
DEVIGNES MD
BERNHEIM A
Citation: Af. Goguel et al., MAPPING OF 22 YACS ON HUMAN-CHROMOSOMES BY FISH USING YEAST DNA ALU-PCR PRODUCTS FOR COMPETITION, Annales de genetique, 39(2), 1996, pp. 64-68
Authors:
DANGLOT G
REGNIER V
FAUVET D
VASSAL G
KUJAS M
BERNHEIM A
Citation: G. Danglot et al., NEUROFIBROMATOSIS-1 (NF1) MESSENGER-RNAS EXPRESSED IN THE CENTRAL-NERVOUS-SYSTEM ARE DIFFERENTIALLY SPLICED IN THE 5' PART OF THE GENE, Human molecular genetics, 4(5), 1995, pp. 915-920
Citation: V. Regnier et al., A TSP509I VARIANT IN EXON-13 OF THE NEUROFIBROMATOSIS TYPE-1 (NF1) GENE ALLOWS THE IDENTIFICATION OF BOTH ALLELES AT THE MESSENGER-RNA LEVEL (VOL 96, PG 131, 1995), Human genetics, 96(6), 1995, pp. 744-744
Citation: V. Regnier et al., A TSP509I VARIANT IN EXON-13 OF THE NEUROFIBROMATOSIS TYPE-1 (NF1) GENE ALLOWS THE IDENTIFICATION OF BOTH ALLELES AT THE MESSENGER-RNA LEVEL, Human genetics, 96(1), 1995, pp. 131-132
Citation: S. Diriong et al., A NEW HYBRID CELL-LINE CONTAINING ONLY HUMAN-CHROMOSOME-15 SELECTED THROUGH FLUORESCENCE IN-SITU HYBRIDIZATION AND CHARACTERIZED BY ALU-PCRAMPLIFICATION OP THE HUMAN DNA, Annales de genetique, 38(1), 1995, pp. 27-31
Authors:
DANGLOT G
TEINTURIER C
DUVERGER A
BERNHEIM A
Citation: G. Danglot et al., TISSUE-SPECIFIC ALTERNATIVE SPLICING OF NEUROFIBROMATOSIS-1 (NF1) MESSENGER-RNA, Biomedicine & pharmacotherapy, 48(8-9), 1994, pp. 365-372
Authors:
LEVY N
LAMOUR V
DANGLOT G
SLIM R
LIPINSKI M
BERNHEIM A
Citation: N. Levy et al., LOCALIZATION OF 15 COSMIDS ON HUMAN CHROMOSOME-22 BY FLUORESCENCE INSITU HYBRIDIZATION, Comptes rendus de l'Academie des sciences. Serie 3, Sciences de la vie, 316(5), 1993, pp. 482-486